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

DRUG INTERACTION ( 15 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
EYE DISORDER ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
VOMITING ( 6 FDA reports)
AGITATION ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
RASH ( 4 FDA reports)
ABASIA ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
APHASIA ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
MONOPARESIS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NODULE ( 3 FDA reports)
PAIN ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HALF-LIFE INCREASED ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFANTILE SPITTING UP ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)

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