About this FactMed analysis covering adverse side effect reports of LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) patients who developed DEPRESSION.

FactMed provides MD-approved analysis to help both patients, researchers, and physicians accurately assess the risk profile for more than 20,000 different pharmaceutical products. The below report offers compiled information from Food & Drug Administration and FactMed user submissions. Between January 2004 and October 2012, 4 individuals taking LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) reported DEPRESSION to the FDA. A total of 39 LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) drug adverse event reaction reports were made with the FDA during this time period. Often the FDA only receives reports of the most critical and severe cases; these numbers may therefore underrepresent the complication rate of the medication.

FDA Research Report

Introduction This page is designed to help you determine the relationship, if any, between LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) and DEPRESSION. In doing so, we compare LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) with other drugs that cause DEPRESSION, to help you evaluate whether or not LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) causes DEPRESSION. Likewise, this page shows the most highly-reported side effects of LOSARTAN POTASSIUM (LOSARTAN POTASSIUM), so you can see if DEPRESSION ranks among LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)'s most well-known side effects.
Summary Statistics
Reports of LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) causing DEPRESSION: 4
Reports of any side effect of LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) : 39
Percentage of LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) patients where DEPRESSION is a reported side effect: 10.2564%

FDA reports of any drug causing DEPRESSION : 98155
Average percentage for all medicated patients where DEPRESSION is reported as a complication: 0.6152%

Physician opinion on LOSARTAN POTASSIUM (LOSARTAN POTASSIUM) as adverse event culprit:

Overall opinion for all reports of this drug:
Most frequent diagnoses/indications for prescribing LOSARTAN POTASSIUM (LOSARTAN POTASSIUM):
HYPERTENSION ( 4 patients )
ILL-DEFINED DISORDER ( 2 patients )
( 0 patients )
Drugs with high FDA adverse event association with DEPRESSION:

FOSAMAX (14302 patients)
VIOXX (14004 patients)
CHANTIX (12075 patients)
ACCUTANE (11815 patients)
SEROQUEL (6501 patients)
ASPIRIN (5780 patients)
ZOLOFT (4557 patients)
XANAX (4245 patients)
NEURONTIN (4113 patients)
AVONEX (3912 patients)
TRASYLOL (3803 patients)
LIPITOR (3699 patients)
PAXIL (3588 patients)
CYMBALTA (3414 patients)
LEXAPRO (3199 patients)
NEXIUM (3185 patients)
ZOMETA (3151 patients)
OXYCONTIN (3045 patients)
SYNTHROID (3026 patients)
AMBIEN (3003 patients)
CELEBREX (2979 patients)
LASIX (2957 patients)
PREDNISONE (2859 patients)
TYSABRI (2704 patients)
LISINOPRIL (2635 patients)
PROZAC (2565 patients)
PRILOSEC (2563 patients)
LYRICA (2563 patients)
EFFEXOR (2438 patients)
WELLBUTRIN (2274 patients)
KLONOPIN (2272 patients)
IBUPROFEN (2167 patients)
PREMARIN (2148 patients)
ALBUTEROL (2143 patients)
SINGULAIR (2115 patients)
LEVAQUIN (2109 patients)
YAZ (2093 patients)
ZOCOR (2068 patients)
VICODIN (2055 patients)
LORAZEPAM (2049 patients)
ATIVAN (2036 patients)
CLONAZEPAM (2016 patients)
ATENOLOL (1992 patients)
COUMADIN (1974 patients)
PREVACID (1962 patients)
AREDIA (1960 patients)
CELEXA (1928 patients)
DURAGESIC-100 (1892 patients)
HYDROCHLOROTHIAZIDE (1877 patients)
PROTONIX (1872 patients)
YASMIN (1852 patients)
EFFEXOR XR (1800 patients)
SIMVASTATIN (1794 patients)
PLAVIX (1748 patients)
REBIF (1642 patients)
NORVASC (1635 patients)
ZYPREXA (1609 patients)
ALPRAZOLAM (1604 patients)
PERCOCET (1603 patients)
FUROSEMIDE (1579 patients)
OMEPRAZOLE (1571 patients)
TOPROL-XL (1565 patients)
LEVOTHYROXINE SODIUM (1563 patients)
FOLIC ACID (1539 patients)
VALIUM (1499 patients)
GABAPENTIN (1470 patients)
ACETAMINOPHEN (1445 patients)
TRAZODONE HCL (1438 patients)
PEGASYS (1419 patients)
RIBAVIRIN (1380 patients)
DIAZEPAM (1376 patients)
LAMICTAL (1334 patients)
FLEXERIL (1330 patients)
HEPARIN (1320 patients)
LORTAB (1304 patients)
HUMIRA (1277 patients)
RISPERDAL (1273 patients)
[THERAPY UNSPECIFIED] (1263 patients)
ADVAIR DISKUS 100/50 (1245 patients)
BEXTRA (1243 patients)
NITROGLYCERIN (1239 patients)
METHOTREXATE (1232 patients)
TOPAMAX (1225 patients)
REMICADE (1213 patients)
FOSAMAX PLUS D (1173 patients)
DIGOXIN (1173 patients)
INSULIN (1167 patients)
POTASSIUM CHLORIDE (1150 patients)
VITAMIN D (1133 patients)
OXYCODONE HCL (1118 patients)
ZYRTEC (1117 patients)
PAROXETINE HCL (1087 patients)
CITALOPRAM HYDROBROMIDE (1085 patients)
AMOXICILLIN (1084 patients)
ALENDRONATE SODIUM (1066 patients)
ENBREL (1061 patients)
CRESTOR (1041 patients)
MIRAPEX (1026 patients)
DIOVAN (1020 patients)
MIRENA (1012 patients)
FENTANYL (1011 patients)
DEPAKOTE (1009 patients)
METFORMIN HCL (1000 patients)
AVANDIA (993 patients)
PEG-INTRON (991 patients)
ELAVIL (989 patients)
ALLEGRA (982 patients)
ZANTAC (981 patients)
FLUOXETINE (965 patients)
CALCIUM (957 patients)
TYLENOL (CAPLET) (930 patients)
MULTI-VITAMINS (922 patients)
ABILIFY (920 patients)
HYDROCODONE (919 patients)
MORPHINE (912 patients)
SEROQUEL XR (911 patients)
METOCLOPRAMIDE (909 patients)
PRISTIQ (900 patients)
BETASERON (896 patients)
GLUCOPHAGE (894 patients)
DEXAMETHASONE (893 patients)
ZITHROMAX (888 patients)
METOPROLOL TARTRATE (881 patients)
BACLOFEN (868 patients)
LOPRESSOR (863 patients)
MIRTAZAPINE (858 patients)
REGLAN (856 patients)
TYLENOL (855 patients)
HYDROCODONE BITARTRATE (855 patients)
CALCIUM (UNSPECIFIED) (854 patients)
ACTONEL (851 patients)
CLARITIN (840 patients)
ZOFRAN (835 patients)
ULTRAM (829 patients)
AMITRIPTYLINE HCL (824 patients)
PREMPRO (820 patients)
REMERON (815 patients)
LANTUS (814 patients)
CHAMPIX (810 patients)
FORTEO (807 patients)
PREDNISONE TAB (807 patients)
GEODON (804 patients)
VITAMIN E (803 patients)
ALLOPURINOL (801 patients)
NUVARING (800 patients)
COREG (797 patients)
TRAMADOL HCL (792 patients)
NAPROXEN (791 patients)
MOTRIN (761 patients)
SOMA (760 patients)
COPEGUS (754 patients)
BONIVA (740 patients)
BENADRYL (736 patients)
CIPROFLOXACIN (733 patients)
RANITIDINE (725 patients)
PEPCID (717 patients)
FLONASE (715 patients)
VITAMINS (UNSPECIFIED) (711 patients)
COZAAR (709 patients)
ACETYLSALICYLIC ACID SRT (707 patients)
TEGRETOL (704 patients)
PROMETHAZINE (702 patients)
SUBOXONE (702 patients)
METOPROLOL (702 patients)
CEPHALEXIN (699 patients)
CLONIDINE (699 patients)
ARIMIDEX (699 patients)
KEPPRA (697 patients)
TEMAZEPAM (697 patients)
ASCORBIC ACID (693 patients)
LITHIUM CARBONATE (689 patients)
ZETIA (688 patients)
SERTRALINE HYDROCHLORIDE (674 patients)
HEPARIN SODIUM INJECTION (668 patients)
MULTI-VITAMIN (667 patients)
OXYCODONE (652 patients)
DECADRON (651 patients)
RITALIN (649 patients)
WELLBUTRIN XL (648 patients)
VANCOMYCIN (647 patients)
TAMOXIFEN CITRATE (645 patients)
WARFARIN SODIUM (631 patients)
VITAMIN B-12 (627 patients)
SPIRONOLACTONE (627 patients)
COMPAZINE (624 patients)
LOVENOX (613 patients)
CLINDAMYCIN (604 patients)
SPIRIVA (603 patients)
ALTACE (602 patients)
METFORMIN (600 patients)
AMNESTEEM (599 patients)
FEMARA (594 patients)
DILAUDID (592 patients)
RESTORIL (591 patients)
COLACE (587 patients)
BUPROPION HCL (586 patients)
VERSED (582 patients)
ACTOS (581 patients)
TRILEPTAL (576 patients)
LEVOXYL (571 patients)
KEFLEX (568 patients)
VIAGRA (564 patients)
GLYBURIDE (561 patients)
ZESTRIL (558 patients)
REBETOL (557 patients)
PROVIGIL (556 patients)
MAGNEVIST (555 patients)
PROTAMINE SULFATE (552 patients)
DROSPIRENONE AND ETHINYL ESTRADIOL (551 patients)
ACIPHEX (550 patients)
Most common side effects for patients taking LOSARTAN POTASSIUM (LOSARTAN POTASSIUM):
DRUG INEFFECTIVE (8 patients)
PAIN (6 patients)
GAIT DISTURBANCE (5 patients)
MYALGIA (5 patients)
ALOPECIA (4 patients)
ASTHENIA (4 patients)
BLOOD CREATINE PHOSPHOKINASE INCREASED (4 patients)
BLOOD LACTATE DEHYDROGENASE INCREASED (4 patients)
BLOOD UREA INCREASED (4 patients)
BRADYCARDIA (4 patients)
COUGH (4 patients)
DEPRESSION (4 patients)
HAEMOLYTIC ANAEMIA (4 patients)
INTERSTITIAL LUNG DISEASE (4 patients)
PULMONARY OEDEMA (4 patients)
PYREXIA (4 patients)
CONDITION AGGRAVATED (3 patients)
CONSTIPATION (3 patients)
CORONARY ARTERY OCCLUSION (3 patients)
DYSPHAGIA (3 patients)
DYSPNOEA (3 patients)
FATIGUE (3 patients)
HEADACHE (3 patients)
PALPITATIONS (3 patients)
PNEUMONIA (3 patients)
SINUS BRADYCARDIA (3 patients)
VENTRICULAR EXTRASYSTOLES (3 patients)
WEIGHT INCREASED (3 patients)
ABASIA (2 patients)
ALDOLASE INCREASED (2 patients)
ANAEMIA (2 patients)
ANTINUCLEAR ANTIBODY POSITIVE (2 patients)
APPETITE DISORDER (2 patients)
BLOOD CREATININE INCREASED (2 patients)
BLOOD POTASSIUM INCREASED (2 patients)
BLOOD PRESSURE DECREASED (2 patients)
BLOOD PRESSURE INCREASED (2 patients)
BODY TEMPERATURE DECREASED (2 patients)
CANDIDA SEROLOGY POSITIVE (2 patients)
CARDIOMEGALY (2 patients)
CHILLS (2 patients)
CYANOSIS (2 patients)
DIALYSIS (2 patients)
DIFFICULTY IN WALKING (2 patients)
DISSEMINATED INTRAVASCULAR COAGULATION (2 patients)
DIZZINESS (2 patients)
ELECTROCARDIOGRAM ABNORMAL (2 patients)
FEELING ABNORMAL (2 patients)
GENERALISED OEDEMA (2 patients)
HAEMODIALYSIS (2 patients)
HEMIPLEGIA (2 patients)
HYPERTENSION (2 patients)
HYPOTENSION (2 patients)
IMPETIGO (2 patients)
LOSS OF CONSCIOUSNESS (2 patients)
LYMPHOCYTE STIMULATION TEST POSITIVE (2 patients)
MARROW HYPERPLASIA (2 patients)
MEDICATION ERROR (2 patients)
MULTIPLE DRUG OVERDOSE (2 patients)
MYOGLOBIN URINE PRESENT (2 patients)
NAUSEA (2 patients)
PAIN IN EXTREMITY (2 patients)
PLEURAL EFFUSION (2 patients)
RENAL DISORDER (2 patients)
RENAL IMPAIRMENT (2 patients)
SEPSIS (2 patients)
SHOCK (2 patients)
SUICIDE ATTEMPT (2 patients)
URINARY RETENTION (2 patients)
VOCAL CORD PARALYSIS (2 patients)
VOMITING (2 patients)
WHITE BLOOD CELL COUNT INCREASED (2 patients)
ABNORMAL SENSATION IN EYE (1 patients)
ALANINE AMINOTRANSFERASE INCREASED (1 patients)
ANGINA UNSTABLE (1 patients)
ANTICONVULSANT DRUG LEVEL DECREASED (1 patients)
ANURIA (1 patients)
ANXIETY (1 patients)
AORTIC DILATATION (1 patients)
APHASIA (1 patients)
ARRHYTHMIA (1 patients)
ARTERIOVENOUS MALFORMATION (1 patients)
ASPARTATE AMINOTRANSFERASE INCREASED (1 patients)
ATRIAL FIBRILLATION (1 patients)
BACK PAIN (1 patients)
BEDRIDDEN (1 patients)
BLOOD GLUCOSE INCREASED (1 patients)
BLOOD PRESSURE DIASTOLIC DECREASED (1 patients)
BLOOD PRESSURE IMMEASURABLE (1 patients)
BLOOD PRESSURE INADEQUATELY CONTROLLED (1 patients)
BLOOD TRIGLYCERIDES ABNORMAL (1 patients)
BREAST CANCER (1 patients)
BURNING SENSATION (1 patients)
BURSA DISORDER (1 patients)
C-REACTIVE PROTEIN INCREASED (1 patients)
CARDIAC FIBRILLATION (1 patients)
CELLULITIS (1 patients)
CEREBRAL HAEMORRHAGE (1 patients)
CEREBRAL INFARCTION (1 patients)
CHONDROMALACIA (1 patients)
CHROMATOPSIA (1 patients)
COMA (1 patients)
CONVULSION (1 patients)
CORONARY ARTERY DISEASE (1 patients)
CORONARY ARTERY STENOSIS (1 patients)
CYSTITIS ESCHERICHIA (1 patients)
DELUSION (1 patients)
DIABETES MELLITUS INADEQUATE CONTROL (1 patients)
DIABETES MELLITUS NON-INSULIN-DEPENDENT (1 patients)
DIVERTICULITIS (1 patients)
DRUG EFFECT DECREASED (1 patients)
DRUG LEVEL BELOW THERAPEUTIC (1 patients)
DRUG LEVEL DECREASED (1 patients)
DRY MOUTH (1 patients)
ELECTROCARDIOGRAM QT PROLONGED (1 patients)
EMOTIONAL DISTRESS (1 patients)
ERYTHEMA (1 patients)
FLAT AFFECT (1 patients)
FULL BLOOD COUNT DECREASED (1 patients)
GOUT (1 patients)
HAEMODYNAMIC INSTABILITY (1 patients)
HEART RATE DECREASED (1 patients)
HEART RATE INCREASED (1 patients)
HEPATITIS (1 patients)
HEPATOCELLULAR DAMAGE (1 patients)
HUNGER (1 patients)
HYPERTENSIVE CRISIS (1 patients)
HYPOGLYCAEMIA UNAWARENESS (1 patients)
HYPOKALAEMIA (1 patients)
HYPOXIA (1 patients)
INTENTIONAL OVERDOSE (1 patients)
INTERNATIONAL NORMALISED RATIO INCREASED (1 patients)
JUGULAR VEIN DISTENSION (1 patients)
LEUKOPENIA (1 patients)
LIVER FUNCTION TEST ABNORMAL (1 patients)
MALAISE (1 patients)
MENINGIOMA MALIGNANT (1 patients)
METRORRHAGIA (1 patients)
MOBILITY DECREASED (1 patients)
MULTIPLE SCLEROSIS (1 patients)
MYOCARDIAL INFARCTION (1 patients)
MYOGLOBIN BLOOD INCREASED (1 patients)
NECK PAIN (1 patients)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL (1 patients)
OEDEMA PERIPHERAL (1 patients)
ORTHOSTATIC HYPOTENSION (1 patients)
OSSICLE DISORDER (1 patients)
OSTEOARTHRITIS (1 patients)
PAIN EXACERBATED (1 patients)
PAIN OF SKIN (1 patients)
PANCYTOPENIA (1 patients)
PARAESTHESIA (1 patients)
PARKINSON'S DISEASE (1 patients)
PERIARTHRITIS (1 patients)
PERIPHERAL CIRCULATORY FAILURE (1 patients)
PHARYNGOLARYNGEAL PAIN (1 patients)
PLATELET AGGREGATION (1 patients)
PLATELET COUNT DECREASED (1 patients)
PLATELET COUNT INCREASED (1 patients)
POLYURIA (1 patients)
PROCEDURAL COMPLICATION (1 patients)
PROTHROMBIN TIME PROLONGED (1 patients)
PRURITUS (1 patients)
PRURITUS GENERALISED (1 patients)
PULMONARY HYPERTENSION (1 patients)
PULSE ABSENT (1 patients)
RENAL FUNCTION TEST ABNORMAL (1 patients)
RESPIRATORY ARREST (1 patients)
SALIVARY HYPERSECRETION (1 patients)
SENILE DEMENTIA (1 patients)
SENSATION OF PRESSURE (1 patients)
SICK SINUS SYNDROME (1 patients)
SINUS ARRHYTHMIA (1 patients)
STOMACH DISCOMFORT (1 patients)
TENDON INJURY (1 patients)
THROAT TIGHTNESS (1 patients)
TINNITUS (1 patients)
TOOTH EXTRACTION (1 patients)
TORSADE DE POINTES (1 patients)
TREMOR (1 patients)
UNEXPECTED THERAPEUTIC DRUG EFFECT (1 patients)
URINARY INCONTINENCE (1 patients)
XANTHOPSIA (1 patients)

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