Please choose an event type to view the corresponding MedsFacts report:

DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
DEHYDRATION ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
AGITATION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
FALL ( 2 FDA reports)
MALAISE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
RETINAL DETACHMENT ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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